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The transcription factor FOXL2 in ovarian function and dysfunction
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Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome
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Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction
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- Journal Article
- A1
- open access
Foxl2 gene and the development of the ovary : a story about goat, mouse, fish and woman
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Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in Blepharophimosis syndrome
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FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation
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Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation